FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

SLIDE CULTURE U 'EIKEN'

K Number: K861631 · Decision Jun 10, 1986
Classifications
1
FEI Numbers
27
Registration Numbers
27
Same Product Code
43
Applicant Total
34
Review Days
42

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Basic Information

Device Name
SLIDE CULTURE U 'EIKEN'
K Number
K861631
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.2660
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
Syn-Kit, Inc.
Date Received
April 29, 1986
Decision Date
June 10, 1986
Product Code
JXA
Advisory Committee
Microbiology
Review Advisory Committee
MI
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
JXA Kit, Screening, Urine

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (JXA), ordered by most recent decision date.

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Other Clearances by Syn-Kit, Inc.

K Number Device Name
K861098 SEROIDEN STREPTO KIT 'EIKEN'
K854819 CPR SLIDE EIKEN
K854820 RA 80 EIKEN
K853276 ASO SLIDE EIKEN
K843758 UROPAPER EIKEN GK
K843753 UROPAPER EIKEN GP
K843754 UROPAPER EIKEN 7
K843760 UROPAPER EIKEN G
K843756 UROPAPER EIKEN 5
K843759 UROPAPER EIKEN HAG
Search all 34 clearances from Syn-Kit, Inc. →